Canonical Allele Identifier: CA1465408636
Gene: GNRHR HGNC NCBI

Linked Data

dbSNP Id: rs1731628810
gnomAD v4: 4-67740093-C-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.67740093C>T , CM000666.2:g.67740093C>T GRCh38
NC_000004.11:g.68605811C>T , CM000666.1:g.68605811C>T GRCh37
NC_000004.10:g.68288406C>T NCBI36
NG_009293.1:g.20994G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000226413.5:c.*387G>A MANE Select ENSP00000226413.5:n.*387G>A
ENST00000226413.4:c.*387G>A ENSP00000226413.4:n.*387G>A
NM_000406.2:c.*387G>A NP_000397.1:n.*387G>A
NM_001012763.1:c.*496G>A NP_001012781.1:n.*496G>A
NM_000406.3:c.*387G>A MANE Select NP_000397.1:n.*387G>A
NM_001012763.2:c.*496G>A NP_001012781.1:n.*496G>A
Search 100 bp 5'
Search 100 bp 3'